U. Altunoğlu Et Al. , "B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies," European Human Genetics Conference , vol.31, Glasgow, England, pp.524, 2023
Altunoğlu, U. Et Al. 2023. B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies. European Human Genetics Conference , (Glasgow, England), 524.
Altunoğlu, U., Kaya, M., Kalaycı, T., & Uyguner, Z. O., (2023). B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies . European Human Genetics Conference (pp.524). Glasgow, England
Altunoğlu, Umut Et Al. "B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies," European Human Genetics Conference, Glasgow, England, 2023
Altunoğlu, Umut Et Al. "B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies." European Human Genetics Conference , Glasgow, England, pp.524, 2023
Altunoğlu, U. Et Al. (2023) . "B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies." European Human Genetics Conference , Glasgow, England, p.524.
@conferencepaper{conferencepaper, author={Umut Altunoğlu Et Al. }, title={B Homozygous NRP1 truncating variant in a multiplex family with conotruncal heart defects, lymphatic malformations and genitourinary anomalies}, congress name={European Human Genetics Conference}, city={Glasgow}, country={England}, year={2023}, pages={524} }